ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2579952535
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.8551644286
Score
0.0460382693
Score
-0.801811812
Score
0.372120569
Score
-0.2243489828
Linked Data - NCBI & NCI
ClinVar Allele:
574629
ClinVar RCV:
RCV000685555
ClinVar Variation:
565884
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Val272Ala
CA397836997
NM_000546.6:c.815T>C